In the PWS Advocacy Space
In most cases, there are no bells and whistles or headline banners that announce much…
Read ArticleIn most cases, there are no bells and whistles or headline banners that announce much…
Read Article“Sport is very important, it’s good for your health, it’s not that you can’t do…
Read Article‘Transition‘ is often the forgotten word when discussing the life cycle of someone living with…
Read ArticleBelow is a summary of some recently published PWS-related research. Source: fpwr.org Vision problems in…
Read ArticleWe’re out of lockdown, the sun is shining, Christmas is around the corner and it’s…
Read ArticlePWSA Vic Mentor Pilot Program Earlier in 2020, the Prader-Willi Syndrome Association Victoria (PWSA Vic)…
Read ArticleWe invite all current Prader-Willi Syndrome Association of Victoria (PWSA Victoria) members to our upcoming…
Read ArticleCalling for expressions of interest Living with Prader-Willi Syndrome is challenging for the individuals but can be…
Read ArticleHayley, our 35-year-old daughter, was born before genetic testing for Prader-Willi Syndrome (PWS) existed and…
Read ArticleCamp Toolangi, September 25th 10am (Saturday) to September 28th (Tuesday) It seems like a lifetime since…
Read Article